Medical device recalls Moderate risk

Abbott Medical Optics Inc. (AMO) recalls Healon GV, Part No. 10294701, 10294801, 10200014, 10201014, 10202014, 10203014

Recall date
April 1, 2017
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-2063-2017
FDA classification
Class II
Brand / firm
Abbott Medical Optics Inc. (AMO)
Sold / distributed
US and worldwide: Austria Belgium Croatia Czech Republic Denmark Finland France Germany Great Britain Iceland Ireland Israel Italy Latvia Lebanon Lithuania Netherlands Norway Portugal Spain Sweden Switzerland Tunisia Turkey Russian Fed Guadeloupe Sri Lanka Australia China Hong Kong Indonesia Malays…

Why it was recalled

Remote possibility that certain solutions in these lots may contain microscopic glass particles due to damage that occurred at the cylinder neck during the manufacturing process.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Healon GV, Part No. 10294701, 10294801, 10200014, 10201014, 10202014, 10203014

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